21 C.F.R. · Food and Drugs
21 C.F.R. § 1.680

How and when will FDA monitor eligible entities?

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Regulatory Text

21 C.F.R. § 1.680 — How and when will FDA monitor eligible entities?

§ 1.680 How and when will FDA monitor eligible entities? FDA may, at any time, conduct an onsite audit of an eligible entity that has received food or facility certification from an accredited third-party certification body under this subpart. Where FDA determines necessary or appropriate, the unannounced audit may be conducted with or without the accredited third-party certification body or the recognized accreditation body (where applicable) present. An FDA audit conducted under this section will be conducted on an unannounced basis and may be preceded by a request for a 30-day operating schedule.

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 1.680
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The regulatory text of 21 C.F.R. § 1.680 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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boisestandard.org United States Law CFR Title 21 21 C.F.R. § 1.680